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Anne F Buckley

Showing results (21-30 of 43) with videos related to

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The Journal of Clinical Investigation|April 7, 2015
Gq signaling causes glomerular injury by activating TRPC6Liming Wang, Grant Jirka, Paul B Rosenberg, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 21, 2014
Adjunctive albuterol enhances the response to enzyme replacement therapy in late-onset Pompe diseaseDwight D Koeberl, Stephanie Austin, Laura E Case, et al.
Molecular Therapy. Methods & Clinical Development|April 8, 2020
Skeletal Muscle Is an Antigen Reservoir in Integrase-Defective Lentiviral Vector-Induced Long-Term ImmunityYi-Yu Lin, Ian Belle, Maria Blasi, et al.
Oncotarget|October 26, 2022
Addendum: Resolution of radiation necrosis with bevacizumab following radiation therapy for primary CNS lymphomaEugene J Vaios, Kristen A Batich, Anne F Buckley, et al.
Pediatric Neurosurgery|May 5, 2022
Successful Neonatal, Intraoperative Neuromonitoring in the Surgical Correction of a Thoracic Dermal Sinus Tract: Technical NoteChidyaonga Shalita, Eric W Sankey, Stephen M Bergin, et al.
Oncotarget|April 1, 2022
Resolution of radiation necrosis with bevacizumab following radiation therapy for primary CNS lymphomaEugene J Vaios, Kristen A Batich, Anne F Buckley, et al.
Orphanet Journal of Rare Diseases|June 22, 2013
Skeletal muscle pathology of infantile Pompe disease during long-term enzyme replacement therapySean N Prater, Trusha T Patel, Anne F Buckley, et al.
Journal of Neuropathology and Experimental Neurology|March 3, 2023
Outside the fiber: Endomysial stromal and capillary pathology in skeletal muscle may impede infusion therapy in infantile-onset Pompe diseaseAnne F Buckley, Ankit K Desai, Christine I Ha, et al.
JIMD Reports|May 5, 2016
Severe Cardiomyopathy as the Isolated Presenting Feature in an Adult with Late-Onset Pompe Disease: A Case ReportMari Mori, Lauren A Bailey, Januario Estrada, et al.
Journal of Inherited Metabolic Disease|August 13, 2017
PRKAG2 mutations presenting in infancyRachel D Torok, Stephanie L Austin, Chanika Phornphutkul, et al.
Pageof 5

Showing results (21-30 of 43) with videos related to

Sort By:
Pageof 5
The Journal of Clinical Investigation|April 7, 2015
Gq signaling causes glomerular injury by activating TRPC6Liming Wang, Grant Jirka, Paul B Rosenberg, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 21, 2014
Adjunctive albuterol enhances the response to enzyme replacement therapy in late-onset Pompe diseaseDwight D Koeberl, Stephanie Austin, Laura E Case, et al.
Molecular Therapy. Methods & Clinical Development|April 8, 2020
Skeletal Muscle Is an Antigen Reservoir in Integrase-Defective Lentiviral Vector-Induced Long-Term ImmunityYi-Yu Lin, Ian Belle, Maria Blasi, et al.
Oncotarget|October 26, 2022
Addendum: Resolution of radiation necrosis with bevacizumab following radiation therapy for primary CNS lymphomaEugene J Vaios, Kristen A Batich, Anne F Buckley, et al.
Pediatric Neurosurgery|May 5, 2022
Successful Neonatal, Intraoperative Neuromonitoring in the Surgical Correction of a Thoracic Dermal Sinus Tract: Technical NoteChidyaonga Shalita, Eric W Sankey, Stephen M Bergin, et al.
Oncotarget|April 1, 2022
Resolution of radiation necrosis with bevacizumab following radiation therapy for primary CNS lymphomaEugene J Vaios, Kristen A Batich, Anne F Buckley, et al.
Orphanet Journal of Rare Diseases|June 22, 2013
Skeletal muscle pathology of infantile Pompe disease during long-term enzyme replacement therapySean N Prater, Trusha T Patel, Anne F Buckley, et al.
Journal of Neuropathology and Experimental Neurology|March 3, 2023
Outside the fiber: Endomysial stromal and capillary pathology in skeletal muscle may impede infusion therapy in infantile-onset Pompe diseaseAnne F Buckley, Ankit K Desai, Christine I Ha, et al.
JIMD Reports|May 5, 2016
Severe Cardiomyopathy as the Isolated Presenting Feature in an Adult with Late-Onset Pompe Disease: A Case ReportMari Mori, Lauren A Bailey, Januario Estrada, et al.
Journal of Inherited Metabolic Disease|August 13, 2017
PRKAG2 mutations presenting in infancyRachel D Torok, Stephanie L Austin, Chanika Phornphutkul, et al.
Pageof 5